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FDA 510(k)

EUROCHIMA SERUM PROTEIN ELECTROPHORESIS METHOD

K-Number: K844710 · 1985-01-07

ApplicantLogos Scientific, Inc.
Decision Date1985-01-07
Product CodeJJN
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EUROCHIMA SERUM PROTEIN ELECTROPHORESIS METHOD is the device name listed in this FDA 510(k) record. The listed applicant is Logos Scientific, Inc.. It received FDA 510(k) clearance on 1985-01-07 under 510(k) number K844710. The device is classified under product code JJN. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EUROCHIMA SERUM PROTEIN ELECTROPHORESIS METHOD?

EUROCHIMA SERUM PROTEIN ELECTROPHORESIS METHOD is a medical device that received FDA 510(k) clearance on 1985-01-07. The listed applicant is Logos Scientific, Inc.. The 510(k) number is K844710.

When did EUROCHIMA SERUM PROTEIN ELECTROPHORESIS METHOD receive FDA 510(k) clearance?

EUROCHIMA SERUM PROTEIN ELECTROPHORESIS METHOD received FDA 510(k) clearance on 1985-01-07, under 510(k) number K844710.

Who is the listed applicant for EUROCHIMA SERUM PROTEIN ELECTROPHORESIS METHOD?

The FDA 510(k) record lists Logos Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EUROCHIMA SERUM PROTEIN ELECTROPHORESIS METHOD?

The FDA product code for EUROCHIMA SERUM PROTEIN ELECTROPHORESIS METHOD is JJN.

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Other records listing Logos Scientific, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K902614ELVI 828 DIGICLOT MULTISCANK843375ELVI 655 FLAME PHOTOMETERK843296ELVI 675 DIGITRONK842313ELVI 146 SEROSCANK842056ELVI 165 PROTEO SEROSKOPK841804ELVI 70 SAFETY CHAMBER

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Related Devices (Code: JJN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K924021POWER SUPPLYThe Binding Site, Ltd.K924020ELECTROPHORESIS TANKThe Binding Site, Ltd.K882344ELECTR-TRANSBLOTTERThe W.E.P. Co.K881852REP SP ELECTROPHORESIS SYSTEM CAT NO. 3170Helena LaboratoriesK882163HELENA REP GEL PROCESSORHelena LaboratoriesK873352RAPID ELECTROPHORESIS SYSTEM (REP)Helena Laboratories

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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